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"arachnoid of spinal cord"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • spastic spinal paraplegia
    ¿¬Ã༺ ô¼ö ´ë¸¶ºñ.
  • spastic spinal paraplegia
    ¿¬Ã༺ ô¼ö ´ë¸¶ºñ(¡­´ë Ø«Ýö)
  • spinal
    ô¼ö(ô±âÐ)ÀÇ, ôÃß(ô±õÐ)ÀÇ.
  • spinal abscess
    ô¼ö³ó¾ç(¡­ÒÛåË).
  • spinal abscess
    ô¼ö³ó¾ç(ô±âÐÒÛåË)
  • spinal absolute alcohol block =subarachnoid a. a. b.
    ôÃß¹«¼ö¾ËÄÝÂ÷´Ü(ô±õÐÙíâ©¡­ó´Ó¨).
  • spinal accessory nerve
    ôÃߺνŰæ
  • spinal amaurosis ³ª amaurosis spinalis
    ô¼ö¼º Èæ³»Àå(¡­àõýÙÒ®î¡)
  • spinal analgesia
    ôÃßÁøÅë(¹ý), ôÃ߸¶Ãë(ô±õÐØ«ö­).
  • spinal animal
    ô¼öµ¿¹°(ô±âÐÔÑÚª).
  • spinal apoplexy
    ô¼öÁ¹Áß(¡­ðïñé).
  • spinal apoplexy
    ô¼öÁ¹Áß(¡­ðïñé)
  • spinal artery
    ô¼öµ¿¸Æ(¡­ÔÑØæ).
  • spinal atatic gait
    ô¼ö¼º ½ÇÁ¶¼º º¸Çà(¡­ã÷ðààõÜÆú¼)
  • spinal ataxia
    ô¼ö¼º ¿îµ¿½ÇÁ¶(Áõ)(¡­àõê¡ÔÑã÷ðàñø).
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 12
PSP pancreatic spasmolytic peptide; paralytic shellfish poisoning; parathyroid secretory protein; period...
SAPF simultaneous anterior and posterior [spinal] fusion
SBMA spinal bulbar muscular atrophy
SCT secretin; sex chromatin test; sexual compatibility test; sickle-cell trait; sperm cytotoxicity; spin...
SCTx spinal cervical traction
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SNB spinal nucleus of the bulbocavernosus
SSR spinal stretch reflex
STN spinal trigeminal nucleus
SBS spino-bulbo-spinal
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 12
spinal veins The veins that drain the spinal cord; they form a plexus on the surface of the cord from which veins pass along the spinal roots to the internal vertebral venous plexus.
Synonym: venae spinales.
(05 Mar 2000)
differential spinal anaesthesia A form of diagnostic spinal anaesthesia producing blockade of different types of nerves in the subarachnoid space, based upon their differences in sensitivity to local anaesthetics; also observed during surgical spinal anaesthesia.
(05 Mar 2000)
dorsal primary ramus of spinal nerve <anatomy, nerve> The smaller, posteriorly-directed major terminal branch (with the ventral primary ramus) of all 31 pairs of mixed spinal nerves, formed at the intervertebral foramen and turning abruptly posteriorly to divide into lateral and medial branches, both of which will supply the deep (true) muscles of the back. The medial branch (rami medialis ) of the dorsal primary ramus also supplies articular branches to the zygopophyseal joints and the periosteum of the vertebral arch. In the neck and upper back, the medial branch continues through the deep and superficial back muscles to supply overlying skin; in the lower back, the lateral branch does this. Nomina Anatomica lists dorsal primary rami as "rami dorsales" for each group of spinal nerves: 1) cervical (nervorum cervicalium ), 2) thoracic (nervorum thoracicorum ), 3) lumbar (nervorum lumbalium ), 4) sacral (nervorum sacralium ), and 5) coccygeal (nervi coccygei ).
Synonym: ramus dorsalis nervorum spinalium, ramus dorsalis, rami posteriores nervorum spinalium, dorsal branch, posterior primary division.
(05 Mar 2000)
infantile progressive spinal muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
infantile spinal muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
isobaric spinal anaesthesia Spinal anaesthesia of same density as cerobrospinal fluid so that the level of anaesthesia is not influenced by a change in the position of the patient.
(05 Mar 2000)
thoracic spinal nerves Twelve nerves on each side, mixed motor and sensory, supplying the muscles and skin of the thoracic and abdominal walls.
Synonym: nervi thoracici.
(05 Mar 2000)
total spinal anaesthesia Spinal anaesthesia extensive enough to produce loss of sensation in all extracranial sensory roots.
(05 Mar 2000)
trigeminal nucleus, spinal Nucleus of the spinal tract of the trigeminal nerve. It is divided cytoarchitectonically into three parts: oralis, caudalis (trigeminal caudal nucleus), and interpolaris.
(12 Dec 1998)
equine spinal ataxia A disease of young horses characterised by progressive weakness and incoordination, most evident in the hind legs; it is associated with lesions in the cervical region of the spinal cord and is the result of compression of the spinal cord by malformed cervical vertebrae.
(05 Mar 2000)
Erb spinal paralysis Chronic myelitis of syphilitic origin.
(05 Mar 2000)
erector-spinal reflex A contraction of part of the erector spinae muscle following scratching of the skin on its outer border.
(05 Mar 2000)
tuberculosis, spinal Osteitis or caries of the vertebrae, usually occurring as a complication of tuberculosis of the lungs.
(12 Dec 1998)
juvenile spinal muscular atrophy Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance.
Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease.
(05 Mar 2000)
familial spinal muscular atrophy Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised.
Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy.
(05 Mar 2000)
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